Bergdahl B, Andersson K E
Eur J Clin Pharmacol. 1977 Apr 20;11(4):267-71. doi: 10.1007/BF00607675.
The in vitro stability of methylproscillaridin has been compared with that of proscillaridin, the activities of the glycosides being assayed by the 86Rb-technique. After incubation in gastric juice at pH 1,2, and 3, the activity half life of each glycoside was proportional to pH and was approximately 0.25 h, 2.5 h, and 25 h, respectively. The inactivation rate in pure hydrochloric acid at pH 2 did not differ from that in gastric juice of the same pH. The glycosides were stable in bile and enteric juice. In faeces, methylproscillaridin was stable and proscillaridin was inactivated with a half life of 32 h. It is concluded that the difference in biological availability between the two glycosides cannot be explained by differences in gastrointestinal stability.
已将甲基海葱苷元的体外稳定性与海葱苷元的进行了比较,通过⁸⁶Rb技术测定糖苷的活性。在pH值为1、2和3的胃液中孵育后,每种糖苷的活性半衰期与pH值成正比,分别约为0.25小时、2.5小时和25小时。在pH值为2的纯盐酸中的失活速率与相同pH值的胃液中的失活速率没有差异。糖苷在胆汁和肠液中稳定。在粪便中,甲基海葱苷元稳定,海葱苷元失活,半衰期为32小时。得出结论,两种糖苷之间生物利用度的差异不能用胃肠道稳定性的差异来解释。